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rs28937897

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0
(T;T) 0 common in complete genomics
Make rs28937897(C;C)
Make rs28937897(C;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position20255097
GeneLZTS1
is asnp
is mentioned by
dbSNPrs28937897
ebirs28937897
HLIrs28937897
Exacrs28937897
Varsomers28937897
Maprs28937897
PheGenIrs28937897
hapmaprs28937897
1000 genomesrs28937897
hgdprs28937897
ensemblrs28937897
gopubmedrs28937897
geneviewrs28937897
scholarrs28937897
googlers28937897
pharmgkbrs28937897
gwascentralrs28937897
openSNPrs28937897
23andMers28937897
23andMe allrs28937897
SNP Nexus

SNPshotrs28937897
SNPdbers28937897
MSV3drs28937897
GWAS Ctlgrs28937897
Max Magnitude0
NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP
OMIM606551
DescESOPHAGEAL SQUAMOUS CELL CARCINOMA, SOMATIC
Variant0001
Relatedalso


ClinVar
Risk rs28937897(C;C)
Alt rs28937897(C;C)
Reference rs28937897(T;T)
Significance Pathogenic
Disease Esophageal squamous cell carcinoma
Variation info
Gene LZTS1
CLNDBN Esophageal squamous cell carcinoma, somatic
Reversed 1
HGVS NC_000008.10:g.20112608A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000004467.4,